| Literature DB >> 34331111 |
Xiao-Xiao Wang1,2, Yan Gao1,2, Jie Jin3, Jun-Ning Cao4, Ji-Feng Feng5, Hua-Qing Wang6, Hui-Lai Zhang7, Qing-Qing Cai1,2, Zhi-Ming Li1,2, Wen-Qi Jiang1,2, Hui-Qiang Huang8,9.
Abstract
This study aimed to identify the maximum-tolerated dose (MTD) of cyclophosphamide when combined with bortezomib and fludarabine (B-FC) in a phase 1b trial, and to assess the efficacy and safety of this combination in a phase 2 trial in patients with relapsed or refractory MCL (rrMCL). Forty patients were enrolled between April 8, 2011, and October 10, 2015. The MTD of cyclophosphamide was identified to be 250 mg/m2 days 1-2. At a median follow-up of 31.6 months (13.5-47.4), among 32 patients in phase 2, 10 (31%) had a complete response and 13 (41%) had a partial response. The median progression-free survival was 21 months (95% CI 7.3-34.7), and the median overall survival was 32.4 months (95% CI 17.8-47.0). Grade 3-4 hematologic AEs included neutropenia (27%) and thrombocytopenia (39%). The B-FC regimen has satisfactory responses and manageable toxicities in rrMCL patients (ClinicalTrials.gov NCT01322776).Entities:
Keywords: Bortezomib; Cyclophosphamide; Fludarabine; Mantle cell lymphoma
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Year: 2021 PMID: 34331111 DOI: 10.1007/s00277-021-04619-4
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673